Canonical Allele Identifier: CA2210135459
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16150797_16150798delinsTG , CM000678.2:g.16150797_16150798delinsTG GRCh38
NC_000016.9:g.16244654_16244655delinsTG , CM000678.1:g.16244654_16244655delinsTG GRCh37
NC_000016.8:g.16152155_16152156delinsTG NCBI36
NG_007558.2:g.77674_77675delinsCA
NG_007558.3:g.77820_77821delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.*381-26_*381-25delinsCA ENSP00000483331.2:n.*381-26_*381-25delinsCA
ENST00000205557.12:c.4209-26_4209-25delinsCA MANE Select ENSP00000205557.7:n.4209-26_4209-25delinsCA
ENST00000640696.1:c.1023-26_1023-25delinsCA ENSP00000492197.1:n.1023-26_1023-25delinsCA
ENST00000205557.11:c.4209-26_4209-25delinsCA ENSP00000205557.7:n.4209-26_4209-25delinsCA
ENST00000456970.6:c.3834-26_3834-25delinsCA ENSP00000405002.2:n.3834-26_3834-25delinsCA
ENST00000576204.5:n.1072-26_1072-25delinsCA
ENST00000622290.4:c.*1418-26_*1418-25delinsCA ENSP00000483331.1:n.*1418-26_*1418-25delinsCA
NM_001171.5:c.4209-26_4209-25delinsCA NP_001162.4:n.4209-26_4209-25delinsCA
XM_011522479.1:c.4176-26_4176-25delinsCA XP_011520781.1:n.4176-26_4176-25delinsCA
XM_011522480.1:c.3867-26_3867-25delinsCA XP_011520782.1:n.3867-26_3867-25delinsCA
XM_011522481.1:c.3867-26_3867-25delinsCA XP_011520783.1:n.3867-26_3867-25delinsCA
XR_933134.1:n.538+6507_538+6508delinsTG
NM_001351800.1:c.3867-26_3867-25delinsCA NP_001338729.1:n.3867-26_3867-25delinsCA
NR_147784.1:n.3871-26_3871-25delinsCA
XM_011522479.2:c.4176-26_4176-25delinsCA XP_011520781.1:n.4176-26_4176-25delinsCA
XM_011522481.3:c.3867-26_3867-25delinsCA XP_011520783.1:n.3867-26_3867-25delinsCA
XM_017023212.1:c.4041-26_4041-25delinsCA XP_016878701.1:n.4041-26_4041-25delinsCA
XM_024450261.1:c.4245-26_4245-25delinsCA XP_024306029.1:n.4245-26_4245-25delinsCA
NM_001171.6:c.4209-26_4209-25delinsCA MANE Select NP_001162.5:n.4209-26_4209-25delinsCA